Salicylaldehyde → HCID 57964972, compound

HRID 1931767Notes

Reaction equation

HRID 1931767 reaction equation
FC(F)(F)C(O)=O.[CH3:8][S:9]([C:12]1[CH:33]=[CH:32][C:15]([O:16][C:17]2[N:22]=[CH:21][N:20]=[C:19]3[N:23]([CH:26]4[CH2:31][CH2:30][NH:29][CH2:28][CH2:27]4)[N:24]=[CH:25][C:18]=23)=[CH:14][CH:13]=1)(=[O:11])=[O:10].[CH:34](=O)[C:35]1[C:36](=[CH:38][CH:39]=[CH:40][CH:41]=1)[OH:37].C(N(CC)CC)C.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>ClCCCl>[CH3:8][S:9]([C:12]1[CH:13]=[CH:14][C:15]([O:16][C:17]2[N:22]=[CH:21][N:20]=[C:19]3[N:23]([CH:26]4[CH2:27][CH2:28][N:29]([CH2:34][C:35]5[CH:41]=[CH:40][CH:39]=[CH:38][C:36]=5[OH:37])[CH2:30][CH2:31]4)[N:24]=[CH:25][C:18]=23)=[CH:32][CH:33]=1)(=[O:11])=[O:10]

Participants

6

Reactant 4

HCID 6998SalicylaldehydeHCID 8471TriethylamineHCID 5049666Sodium triacetoxyborohydrideHCID 669153264-(4-methanesulfonyl-phenoxy)-1-piperidin-4-yl-1H-pyrazolo[3,4-d]pyrimidine trifluoroacetate salt2×

Product 1

HCID 57964972HCID 57964972, compound

Reagents, catalysts & solvents 1

HCID 111,2-DichloroethaneSolvent

Procedure

2-{4-[4-(4-Methanesulfonyl-phenoxy)-pyrazolo[3,4-d]pyrimidin-1-yl]-piperidin-1-ylmethyl}-phenol was prepared according to General Procedure H by the reaction of 4-(4-methanesulfonyl-phenoxy)-1-piperidin-4-yl-1H-pyrazolo[3,4-d]pyrimidine trifluoroacetate salt (Intermediate 27) with salicylaldehyde (available from Aldrich Chemical Company, Inc., Milwaukee, Wis., USA), triethylamine, and sodium triacetoxyborohydride in 1,2-dichloroethane. 1H NMR (400 MHz, DMSO-d6) δ 1.95-2.03 (m, 2H), 2.19-2.28 (m, 4H), 2.32-2.38 (m, 2H), 2.98-3.06 (m, 2H), 3.30 (methyl sulfonyl and water peak), 3.71 (s, 2H), 4.84-4.89 (m, 1H), 6.75-6.79 (m, 2H), 7.08-7.14 (m, 2H), 7.63-7.65 (m, 2H), 8.04-8.07 (m, 2H), 8.40 (s, 1H), 8.56 (s, 1H). Mass spectrum MH+=480.

Sources & evidence

ORD record
ord-11fdbebc7a6c4699833f5168757b1bfe
Source dataset
uspto-grants-2012_05
Patent number
US08188098B2

Reaction notes

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